Cerebral Microembolism in the Critically Ill With Acute Kidney Injury
Not Applicable
Terminated
- Conditions
- Cerebral Embolism
- Interventions
- Device: Renal replacement therapy
- Registration Number
- NCT02621749
- Lead Sponsor
- Insel Gruppe AG, University Hospital Bern
- Brief Summary
The primary objective of this study is to investigate the impact of continuous renal replacement therapy and intermittent renal replacement therapy on microbubble / cerebral microemboli generation in a cohort of critically ill patients with dialysis-dependent acute kidney injury.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- TERMINATED
- Sex
- All
- Target Recruitment
- 66
Inclusion Criteria
- > 18 yrs.
- Signed IC
Exclusion Criteria
- Heart disease (PFO, ASD, VSD, severe valvular disease)
- Atrial fibrillation
- Cerebrovascular pathology
- Missing temporal bone window
- Allergy to plastic contained in the investigative device (transcranial Doppler)
- Chronic kidney disease
- Pregnancy
- Participation in another study
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description IRRT group Renal replacement therapy the IRRT group receives intermittent renal replacement therapy after termination of CRRT. CRRT group Renal replacement therapy the CRRT group receives continuous renal replacement therapy for acute kidney injury
- Primary Outcome Measures
Name Time Method Cerebral Microembolic Load detected by Transcranial Doppler Ultrasound During hemodialysis therapy
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
University Hospital Bern
🇨ðŸ‡Bern, Switzerland